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ID30139A - COMPLEX OF RAS-FARNESILTRANSFERASE AND SULFOBUTILETER-7- INHIBITORS OR CYCLODEXTRINS OR 2-HYDROXYXYOPROPYL--SICLODODSTRINTS AND ITS METHODS - Google Patents

COMPLEX OF RAS-FARNESILTRANSFERASE AND SULFOBUTILETER-7- INHIBITORS OR CYCLODEXTRINS OR 2-HYDROXYXYOPROPYL--SICLODODSTRINTS AND ITS METHODS

Info

Publication number
ID30139A
ID30139A IDW00200101596A ID20011596A ID30139A ID 30139 A ID30139 A ID 30139A ID W00200101596 A IDW00200101596 A ID W00200101596A ID 20011596 A ID20011596 A ID 20011596A ID 30139 A ID30139 A ID 30139A
Authority
ID
Indonesia
Prior art keywords
sulfobutileter
siclododstrints
hydroxyxyopropyl
farnesiltransferase
cyclodextrins
Prior art date
Application number
IDW00200101596A
Other languages
Indonesian (id)
Inventor
Krishnaswamy S Baghavan
Timothy M Malloy
Sailesh A Varia
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of ID30139A publication Critical patent/ID30139A/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nanotechnology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • General Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • Medical Informatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Plural Heterocyclic Compounds (AREA)
IDW00200101596A 1999-01-21 1999-12-21 COMPLEX OF RAS-FARNESILTRANSFERASE AND SULFOBUTILETER-7- INHIBITORS OR CYCLODEXTRINS OR 2-HYDROXYXYOPROPYL--SICLODODSTRINTS AND ITS METHODS ID30139A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11664799P 1999-01-21 1999-01-21

Publications (1)

Publication Number Publication Date
ID30139A true ID30139A (en) 2001-11-08

Family

ID=22368422

Family Applications (1)

Application Number Title Priority Date Filing Date
IDW00200101596A ID30139A (en) 1999-01-21 1999-12-21 COMPLEX OF RAS-FARNESILTRANSFERASE AND SULFOBUTILETER-7- INHIBITORS OR CYCLODEXTRINS OR 2-HYDROXYXYOPROPYL--SICLODODSTRINTS AND ITS METHODS

Country Status (33)

Country Link
US (1) US6218375B1 (en)
EP (1) EP1143796A4 (en)
JP (1) JP2002535253A (en)
KR (1) KR100708360B1 (en)
CN (1) CN1219517C (en)
AR (1) AR022323A1 (en)
AU (1) AU772204B2 (en)
BG (1) BG105666A (en)
BR (1) BR9916566A (en)
CA (1) CA2359646C (en)
CO (1) CO5160253A1 (en)
CZ (1) CZ20012601A3 (en)
EE (1) EE200100382A (en)
GE (1) GEP20043214B (en)
HK (1) HK1038865A1 (en)
HU (1) HUP0105160A3 (en)
ID (1) ID30139A (en)
IL (1) IL144025A (en)
LT (1) LT4893B (en)
LV (1) LV12712B (en)
MY (1) MY119700A (en)
NO (1) NO20013585L (en)
NZ (1) NZ511995A (en)
PE (1) PE20001419A1 (en)
PL (1) PL195280B1 (en)
RU (1) RU2230062C2 (en)
SK (1) SK9602001A3 (en)
TR (1) TR200102109T2 (en)
TW (1) TWI232752B (en)
UA (1) UA67825C2 (en)
UY (2) UY25986A1 (en)
WO (1) WO2000042849A1 (en)
ZA (1) ZA200104416B (en)

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TWI310684B (en) 2000-03-27 2009-06-11 Bristol Myers Squibb Co Synergistic pharmaceutical kits for treating cancer
JP2003063965A (en) * 2001-06-13 2003-03-05 Otsuka Pharmaceut Factory Inc Cilostazol aqueous composition for injection
US6566347B1 (en) * 2001-08-22 2003-05-20 Duquesne University Of The Holy Ghost Controlled release pharmaceutical
AU2002359412A1 (en) * 2001-11-13 2003-05-26 Bristol-Myers Squibb Company Process for the preparation of 3,7-disubstituted-2,3,4,5- tetrahydro-1h-1,4-benzodiazepine compounds
KR100451485B1 (en) 2002-03-28 2004-10-06 주식회사종근당 Inclusion compounds of fumagillol derivative or its salt, and pharmaceutical compositions comprising the same
US6869939B2 (en) * 2002-05-04 2005-03-22 Cydex, Inc. Formulations containing amiodarone and sulfoalkyl ether cyclodextrin
WO2003106628A2 (en) * 2002-06-17 2003-12-24 Bristol-Myers Squibb Company Benzodiazepine inhibitors of mitochondial f1f0 atp hydrolase and methods of inhibiting f1f0 atp hydrolase
US7157446B2 (en) * 2003-05-02 2007-01-02 Bristol Myers Squibb Company Complex of ras-farnesyltransferase inhibitor, a cyclodextrin, and ethanol
US20070020299A1 (en) 2003-12-31 2007-01-25 Pipkin James D Inhalant formulation containing sulfoalkyl ether cyclodextrin and corticosteroid
CA2624463C (en) * 2005-09-30 2017-02-14 Ovation Pharmaceuticals, Inc. Novel parenteral carbamazepine formulation
US20100204178A1 (en) 2006-10-02 2010-08-12 James Cloyd Novel parenteral carbamazepine formulation
CN100503647C (en) * 2005-11-02 2009-06-24 南京师范大学 Hydroxypropyl-sulfobutyl-β-cyclodextrin and its preparation method, analysis method and application in pharmacy
TW200806284A (en) * 2006-03-31 2008-02-01 Alcon Mfg Ltd Prenyltransferase inhibitors for ocular hypertension control and the treatment of glaucoma
RU2009123536A (en) * 2006-11-21 2010-12-27 Новартис АГ (CH) Stable parenteral formulations, including benzodiazepine-based PCB inhibitors
SI3106463T1 (en) 2008-10-22 2018-08-31 Array Biopharma, Inc. Substituted pyrazolo(1,5-)pyrimidine compounds as trk kinase inhibitors
JP5798621B2 (en) 2010-05-26 2015-10-21 ニューロフィキシア ベー．フェー． 2-Iminobiotin preparation and use thereof
WO2012034038A2 (en) 2010-09-09 2012-03-15 H. Lee Moffitt Cancer Center And Research Institute, Inc. Dual inhibitors of farnesyltransferase and geranylgeranyltransferase i
JP6165744B2 (en) * 2011-10-07 2017-07-19 パイシーズ セラピューティックス エルエルシーＰｉｓｃｅｓ Ｔｈｅｒａｐｅｕｔｉｃｓ Ｌｌｃ Treatment of malignant and non-malignant diseases with RAS antagonists
CN105194685A (en) * 2015-10-15 2015-12-30 重庆大学 Sulphaguanidine and sulfobutyl ether-beta-cyclodextrin inclusion compound and powder injection preparation
EP3389653B1 (en) 2015-12-16 2023-11-08 Neurophyxia B.V. 2-iminobiotin for use in the treatment of brain cell injury
US10045991B2 (en) 2016-04-04 2018-08-14 Loxo Oncology, Inc. Methods of treating pediatric cancers
JP7061602B2 (en) 2016-04-04 2022-04-28 ロクソ オンコロジー， インコーポレイテッド (S) -N- (5-((R) -2- (2,5-difluorophenyl) -pyrrolidin-1-yl) -pyrazolo [1,5-a] pyrimidin-3-yl) -3-hydroxy Liquid formulation of pyrrolidine-1-carboxamide
UA127826C2 (en) 2016-05-18 2024-01-17 Локсо Онколоджі, Інк. Preparation of (s)-n-(5-((r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-y l)-3-hydroxypyrrolidine-1-carboxamide
JOP20190092A1 (en) 2016-10-26 2019-04-25 Array Biopharma Inc PROCESS FOR THE PREPARATION OF PYRAZOLO[1,5-a]PYRIMIDINES AND SALTS THEREOF
US20210145816A1 (en) * 2019-11-15 2021-05-20 Cyclolab Cyclodextrin Research And Development Laboratory Ltd. Pharmaceutical formulation of lonafarnib with a sulfobutylether beta-cyclodextrin
WO2023113479A1 (en) * 2021-12-15 2023-06-22 Sillajen, Inc. Pharmaceutical compositions comprising modified beta-cyclodextrins
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5630927A (en) * 1979-08-24 1981-03-28 Zeria Shinyaku Kogyo Kk Stabilization of guaiazulene and its derivative
US4371673A (en) * 1980-07-21 1983-02-01 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Water soluble forms of retinoids
US4727064A (en) * 1984-04-25 1988-02-23 The United States Of America As Represented By The Department Of Health And Human Services Pharmaceutical preparations containing cyclodextrin derivatives
US4596795A (en) * 1984-04-25 1986-06-24 The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (en) * 1990-01-23 1999-01-15 . Cyclodextrin derivatives with increased water solubility and uses thereof
JPH07165616A (en) * 1993-12-09 1995-06-27 Hisamitsu Pharmaceut Co Inc Complex composition of cyclodextrin and method for making complex
US6011029A (en) * 1996-02-26 2000-01-04 Bristol-Myers Squibb Company Inhibitors of farnesyl protein transferase
JPH1067639A (en) * 1996-08-26 1998-03-10 Shiseido Co Ltd Vitamin E-Vitamin C phosphoric acid diester / cyclodextrin clathrate and external skin preparation containing the clathrate

Also Published As

Publication number Publication date
UA67825C2 (en) 2004-07-15
CO5160253A1 (en) 2002-05-30
EE200100382A (en) 2002-12-16
CA2359646A1 (en) 2000-07-27
SK9602001A3 (en) 2002-06-04
AR022323A1 (en) 2002-09-04
CN1219517C (en) 2005-09-21
LT2001064A (en) 2001-10-25
UY25987A1 (en) 2000-09-29
US6218375B1 (en) 2001-04-17
PE20001419A1 (en) 2001-02-21
BR9916566A (en) 2001-11-13
NO20013585L (en) 2001-09-04
CZ20012601A3 (en) 2002-05-15
BG105666A (en) 2002-04-30
EP1143796A1 (en) 2001-10-17
TR200102109T2 (en) 2001-12-21
PL195280B1 (en) 2007-08-31
KR100708360B1 (en) 2007-04-17
CN1333651A (en) 2002-01-30
CA2359646C (en) 2008-12-02
UY25986A1 (en) 2000-09-29
LV12712B (en) 2002-01-20
RU2230062C2 (en) 2004-06-10
LV12712A (en) 2001-09-20
AU772204B2 (en) 2004-04-22
NO20013585D0 (en) 2001-07-20
TWI232752B (en) 2005-05-21
JP2002535253A (en) 2002-10-22
KR20010101611A (en) 2001-11-14
IL144025A (en) 2004-05-12
EP1143796A4 (en) 2002-03-20
MY119700A (en) 2005-06-30
LT4893B (en) 2002-02-25
IL144025A0 (en) 2002-04-21
ZA200104416B (en) 2002-05-29
PL366338A1 (en) 2005-01-24
WO2000042849A1 (en) 2000-07-27
HUP0105160A2 (en) 2002-05-29
NZ511995A (en) 2003-11-28
AU2374000A (en) 2000-08-07
HK1038865A1 (en) 2002-04-04
HUP0105160A3 (en) 2003-01-28
GEP20043214B (en) 2004-04-26

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